Canonical Allele Identifier: CA2543807672

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308871_40308873del , CM000674.2:g.40308871_40308873del	GRCh38
NC_000012.11:g.40702673_40702675del , CM000674.1:g.40702673_40702675del	GRCh37
NC_000012.10:g.38988940_38988942del	NCBI36
NG_011709.1:g.88861_88863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4189+175_4189+177del MANE Select	ENSP00000298910.7:n.4189+175_4189+177del
ENST00000679360.1:c.*3098+175_*3098+177del	ENSP00000505368.1:n.*3098+175_*3098+177del
ENST00000680790.1:c.3934+175_3934+177del	ENSP00000505335.1:n.3934+175_3934+177del
ENST00000298910.11:c.4189+175_4189+177del	ENSP00000298910.7:n.4189+175_4189+177del
ENST00000430804.5:c.1485+175_1485+177del
ENST00000479187.5:n.870+175_870+177del
NM_198578.3:c.4189+175_4189+177del	NP_940980.3:n.4189+175_4189+177del
XM_005268629.2:c.4189+175_4189+177del	XP_005268686.1:n.4189+175_4189+177del
XM_011537877.1:c.4189+175_4189+177del	XP_011536179.1:n.4189+175_4189+177del
XM_011537878.1:c.4189+175_4189+177del	XP_011536180.1:n.4189+175_4189+177del
XM_011537879.1:c.2986+175_2986+177del	XP_011536181.1:n.2986+175_2986+177del
XM_011537880.1:c.4189+175_4189+177del	XP_011536182.1:n.4189+175_4189+177del
XM_011537881.1:c.4189+175_4189+177del	XP_011536183.1:n.4189+175_4189+177del
XM_005268629.4:c.4189+175_4189+177del	XP_005268686.1:n.4189+175_4189+177del
XM_011537877.3:c.4189+175_4189+177del	XP_011536179.1:n.4189+175_4189+177del
XM_011537881.3:c.4189+175_4189+177del	XP_011536183.1:n.4189+175_4189+177del
XM_017018786.2:c.4189+175_4189+177del	XP_016874275.1:n.4189+175_4189+177del
XM_017018787.1:c.1105+175_1105+177del	XP_016874276.1:n.1105+175_1105+177del
XM_017018788.2:c.451+175_451+177del	XP_016874277.1:n.451+175_451+177del
XM_024448833.1:c.2986+175_2986+177del	XP_024304601.1:n.2986+175_2986+177del
XR_001748574.2:n.4431+175_4431+177del
NM_198578.4:c.4189+175_4189+177del MANE Select	NP_940980.4:n.4189+175_4189+177del